A Study Evaluating the Impact of P-tau217 Blood Biomarker Testing on Early Evaluation and Management of Patients Presenting With Cognitive Complaint

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorEli Lilly and Company

About this trial

The purpose of the study is to measure the difference in the proportion of participants with prespecified patient management actions between a tested interventional group and a control group.

Eligibility criteria

Qualifiers

Primary care physician (PCPs): physicians such as family medicine practitioners and internists who do not specialize in neurological care.

Secondary care physicians (SCPs): physicians such as geriatricians or neurologists who see patients for specific reasons.

Tertiary care physicians (TCPs): specialty neurologists who focus on certain neurological conditions.

Group 1: PCPs who routinely evaluate and manage patients over the age of 50 in a family practice or internist setting.

Disqualifiers

In the 18 months prior to identification have prior or associated HCP-ordered referral or prior prescription of drug therapies, for the SCIC

Participants with previous amyloid- or tau-specific tests, defined as

Amyloid position emission tomography (PET)

Tau PET

Trial design

Treatments tested in this trial

  • P-tau217
  • Standard of Care

Treatment groups

7,000 Participants
are divided into 2 treatment groups

Sponsors and collaborators